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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Culture Media, For Isolation Of Pathogenic Neisseria
510(k) Number K850841
Device Name MOD THAYER MARTIN MARTIN LEWIS
Applicant
Micro Media Laboratories
2775 Kurtz
San Diego,  CA  92110
Applicant Contact PETER G MARTIN
Correspondent
Micro Media Laboratories
2775 Kurtz
San Diego,  CA  92110
Correspondent Contact PETER G MARTIN
Regulation Number866.2410
Classification Product Code
JTY  
Date Received03/01/1985
Decision Date 03/20/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Microbiology
510k Review Panel Microbiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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